DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
A-POXIDE
FDA Application No:
(ANDA) 085517
Active Ingredient(s):
CHLORDIAZEPOXIDE HYDROCHLORIDE
Company:
ABBOTT
Label History
Labels are not available on this site for APOXIDE, (ANDA) 085517
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
1/25/1984
009
Chemistry
3/31/1982
007
Chemistry
3/31/1982
006
Chemistry
Therapeutic Equivalents
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